What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Biochemistry, Cell biology, Nuclear magnetic resonance spectroscopy, Membrane protein and Biophysics.
Volker Dötsch has included themes like Autophagy, DNA-binding protein, Ubiquitin and Binding site in his Cell biology study.
The concepts of his Nuclear magnetic resonance spectroscopy study are interwoven with issues in Structural biology, Xenopus, Macromolecule and Telomere.
His Membrane protein research is multidisciplinary, incorporating perspectives in Computational biology, Membrane transport, G protein-coupled receptor and Proteomics.
His study in Biophysics is interdisciplinary in nature, drawing from both Electron paramagnetic resonance, Site-directed spin labeling and In vivo.
In his study, which falls under the umbrella issue of Transactivation, Molecular biology is strongly linked to Trans-Activators.
His most cited work include:
- p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. (1793 citations)
- Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth (894 citations)
- Nix is a selective autophagy receptor for mitochondrial clearance (806 citations)
What are the main themes of his work throughout his whole career to date?
Volker Dötsch mainly investigates Biochemistry, Cell biology, Membrane protein, Biophysics and Nuclear magnetic resonance spectroscopy.
His Biochemistry study deals with Stereochemistry intersecting with Peptide sequence.
As part of one scientific family, Volker Dötsch deals mainly with the area of Cell biology, narrowing it down to issues related to the Transcription factor, and often Gene isoform.
His Membrane protein study combines topics from a wide range of disciplines, such as Computational biology and Cell free.
His work carried out in the field of Biophysics brings together such families of science as Plasma protein binding and Protein folding.
His studies in Nuclear magnetic resonance spectroscopy integrate themes in fields like Crystallography, Xenopus, Macromolecule and Analytical chemistry.
He most often published in these fields:
- Biochemistry (35.21%)
- Cell biology (29.58%)
- Membrane protein (23.59%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (29.58%)
- Biophysics (15.85%)
- Phosphorylation (6.69%)
In recent papers he was focusing on the following fields of study:
Volker Dötsch mostly deals with Cell biology, Biophysics, Phosphorylation, Receptor and Ubiquitin.
His Cell biology research integrates issues from Autophagy, Mitophagy, Transcription factor, DNA and Biosensor.
His research in Biophysics intersects with topics in Transporter, Chaperone, Structural biology, Bacterial outer membrane and Membrane.
His Phosphorylation study improves the overall literature in Biochemistry.
Within one scientific family, he focuses on topics pertaining to Neuroscience under Receptor, and may sometimes address concerns connected to Histamine H3 receptor.
His Ubiquitin research includes themes of Enzyme, Hydroxylation, Endoplasmic reticulum and Protein–protein interaction.
Between 2018 and 2021, his most popular works were:
- Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) (38 citations)
- Regulation of Phosphoribosyl-Linked Serine Ubiquitination by Deubiquitinases DupA and DupB. (33 citations)
- Selective autophagy maintains centrosome integrity and accurate mitosis by turnover of centriolar satellites (22 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Cell biology, Biophysics, Ubiquitin, Endoplasmic reticulum and DNA damage.
Volker Dötsch combines subjects such as Homologous chromosome, Meiosis, DNA and PCM1, Centrosome with his study of Cell biology.
His study in Biophysics is interdisciplinary in nature, drawing from both Pharmacophore, Organic cation transport proteins, Fusion protein and Binding site.
The Ubiquitin study combines topics in areas such as Cytosol, ATPase, Enzyme and Protein degradation.
His DNA damage study incorporates themes from Casein kinase 1, Phosphorylation, Regulator, Kinase and Tetramer.
His work deals with themes such as Haematopoiesis, Stem cell, Carcinogenesis, Transcription factor and Wild type, which intersect with Phosphorylation.
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